CLASS I Food recall · Reported 27 Mar 2024 · FDA Enforcement Report
Wesco mint no-bake cookie bites cup recalled by Wesco Central Commissary
Wesco Central Commissary is recalling Wesco mint no-bake cookie bites cup, distributed in Michigan. The recall was initiated on 7 Mar 2024 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1096-2024
- FDA event ID
- 94204
- Recalling firm
- Wesco Central Commissary, North Muskegon, MI
- Brand
- Wesco
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 7 Mar 2024
- FDA classified
- 26 Mar 2024
- Reported
- 27 Mar 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Peanuts
- Product category
- Cookies
Timeline
| 7 Mar 2024 | Recall initiated by company | |
| 26 Mar 2024 | Classified by FDA | +19 days |
| 27 Mar 2024 | Published in enforcement report | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
undeclared peanut and soy not listed in contains statement.
Product as listed by the FDA
Wesco mint no-bake cookie bites 9oz cup UPC 750308040474
Where it was distributed
MI
Questions about this recall
Is Wesco mint no-bake cookie bites cup recalled?
Yes. Wesco Central Commissary recalled Wesco mint no-bake cookie bites cup on 7 Mar 2024. The recall is Class I and its status is Terminated. Recall number F-1096-2024.
Why was it recalled?
undeclared peanut and soy not listed in contains statement.
Which lots are affected?
All. sell by: 03/15/2024, 03/16/2024, 03/17/2024, 03/18/2024
Where was it sold?
MI
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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